Evidence map›Paper›PMID 24049729›Full record

ArticleMolecular metabolism2013

Peripheral activation of the Y2-receptor promotes secretion of GLP-1 and improves glucose tolerance.

Keval Chandarana, Cigdem Gelegen, Elaine E Irvine, Agharul I Choudhury, Chloé Amouyal, Fabrizio Andreelli, Dominic J Withers, Rachel L Batterham

Open access · goldAbstract read
In one paragraph

Article in Molecular metabolism, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.2field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 65 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. PYYNeuropharmacology · 2023
    Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Peptide YYEuropean journal of nutrition · 2020
    Article
  11. Review
  12. Article
  13. Dipeptidyl Peptidase-4 at the Interface Between Inflammation and Metabolism.Clinical medicine insights. Endocrinology and diabetes · 2020
    Review
  14. Calcium Signaling Pathways: Key Pathways in the Regulation of Obesity.International journal of molecular sciences · 2019
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 6 institutions in 2 countries.

Keval ChandaranaCentre for Obesity Research, Department of Medicine, University College London, Rayne Institute, 5 University Street, WC1E 6JJ, London, UK.
Cigdem Gelegen
Elaine E Irvine
Agharul I Choudhury
Chloé Amouyal
Fabrizio Andreelli
Dominic J Withers
Rachel L Batterham
Imperial College London · GBUniversity College London · GBFondation pour l’innovation en Cadiométabolisme et Nutrition · FRInserm · FRMedical Research Council · GBNational Institute for Health Research · GB

Funding

Medical Research Council G108/551Medical Research Council MC_U120097114
6 · The paper itself

Abstract

The effect of peptide tyrosine-tyrosine (PYY) on feeding is well established but currently its role in glucose homeostasis is poorly defined. Here we show in mice, that intraperitoneal (ip) injection of PYY3-36 or Y2R agonist improves nutrient-stimulated glucose tolerance and enhances insulin secretion; an effect blocked by peripheral, but not central, Y2R antagonist administration. Studies on isolated mouse islets revealed no direct effect of PYY3-36 on insulin secretion. Bariatric surgery in mice, enterogastric anastomosis (EGA), improved glucose tolerance in wild-type mice and increased circulating PYY and active GLP-1. In contrast, in Pyy-null mice, post-operative glucose tolerance and active GLP-1 levels were similar in EGA and sham-operated groups. PYY3-36 ip increased hepato-portal active GLP-1 plasma levels, an effect blocked by ip Y2R antagonist. Collectively, these data suggest that PYY3-36 therefore acting via peripheral Y2R increases hepato-portal active GLP-1 plasma levels and improves nutrient-stimulated glucose tolerance.

Indexed as

aCSF, artificial cerebrospinal fluidactive GLP-1, glucagon-like peptide-1(7-36)amideAUC, area under the curveCNS, central nervous systemDPP-4, di-peptidyl peptidase-4EGA, entero-gastric anastomosisGLP-1Glucose homeostasisHFD, high-fat dietICV, intracerebroventricularIPGTT, intraperitoneal glucose tolerance testip, intraperitonealPYYPYY, peptide tyrosine–tyrosineT2DM, type 2 diabetes mellitusWT, wild-typeY2-receptorY2R, Y2-receptor

Identifiers

PMID24049729
PMCPMC3773824
OpenAlexW2048117685

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.